Brusgaard K - Search Results

1

A novel gene in early childhood diabetes: EDEM2 silencing decreases SLC2A2 and PXD1 expression, leading to impaired insulin secretion.

Alhaidan Y, Christesen HT, Højlund K, Al Balwi MA, Brusgaard K. Alhaidan Y, et al. Among authors: brusgaard k. Mol Genet Genomics. 2020 Sep;295(5):1253-1262. doi: 10.1007/s00438-020-01695-5. Epub 2020 Jun 16. Mol Genet Genomics. 2020. PMID: 32556999

2

Effect of insulin on protein phosphatase 2A expression in muscle in type 2 diabetes.

Højlund K, Poulsen M, Staehr P, Brusgaard K, Beck-Nielsen H. Højlund K, et al. Among authors: brusgaard k. Eur J Clin Invest. 2002 Dec;32(12):918-23. doi: 10.1046/j.1365-2362.2002.01098.x. Eur J Clin Invest. 2002. PMID: 12534451

3

The primary defect in glycogen synthase activity is not based on increased glycogen synthase kinase-3alpha activity in diabetic myotubes.

Gaster M, Brusgaard K, Handberg A, Højlund K, Wojtaszewski JF, Beck-Nielsen H. Gaster M, et al. Among authors: brusgaard k. Biochem Biophys Res Commun. 2004 Jul 9;319(4):1235-40. doi: 10.1016/j.bbrc.2004.05.109. Biochem Biophys Res Commun. 2004. PMID: 15194499

4

Reduced expression of nuclear-encoded genes involved in mitochondrial oxidative metabolism in skeletal muscle of insulin-resistant women with polycystic ovary syndrome.

Skov V, Glintborg D, Knudsen S, Jensen T, Kruse TA, Tan Q, Brusgaard K, Beck-Nielsen H, Højlund K. Skov V, et al. Among authors: brusgaard k. Diabetes. 2007 Sep;56(9):2349-55. doi: 10.2337/db07-0275. Epub 2007 Jun 11. Diabetes. 2007. PMID: 17563058 Free article.

5

Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genes.

Frederiksen CM, Højlund K, Hansen L, Oakeley EJ, Hemmings B, Abdallah BM, Brusgaard K, Beck-Nielsen H, Gaster M. Frederiksen CM, et al. Among authors: brusgaard k. Diabetologia. 2008 Nov;51(11):2068-77. doi: 10.1007/s00125-008-1122-9. Epub 2008 Aug 22. Diabetologia. 2008. PMID: 18719883

6

Vitamin D and diabetes: its importance for beta cell and immune function.

Wolden-Kirk H, Overbergh L, Christesen HT, Brusgaard K, Mathieu C. Wolden-Kirk H, et al. Among authors: brusgaard k. Mol Cell Endocrinol. 2011 Dec 5;347(1-2):106-20. doi: 10.1016/j.mce.2011.08.016. Epub 2011 Aug 26. Mol Cell Endocrinol. 2011. PMID: 21889571 Review.

7

Recurrent spontaneous hypoglycaemia causes loss of neurogenic and neuroglycopaenic signs in infants with congenital hyperinsulinism.

Christesen HT, Brusgaard K, Hussain K. Christesen HT, et al. Among authors: brusgaard k. Clin Endocrinol (Oxf). 2012 Apr;76(4):548-54. doi: 10.1111/j.1365-2265.2011.04250.x. Clin Endocrinol (Oxf). 2012. PMID: 21981106

8

[Congenital hyperinsulinism--diagnosis and treatment].

Christesen HT, Bruun MF, Christoffersen SH, Rasmussen L, Petersen H, Detlefsen S, Hovendal CP, Hansen TG, Hansen TP, Brusgaard K. Christesen HT, et al. Among authors: brusgaard k. Ugeskr Laeger. 2011 Nov 21;173(47):3020-5. Ugeskr Laeger. 2011. PMID: 22118585 Review. Danish.

9

[Congenital hyperinsulinism--new causes and clinical variations].

Bruun MF, Christoffersen SH, Brusgaard K, Detlefsen S, Christesen HT. Bruun MF, et al. Among authors: brusgaard k. Ugeskr Laeger. 2011 Nov 21;173(47):3026-31. Ugeskr Laeger. 2011. PMID: 22118586 Review. Danish.

10

Unraveling the effects of 1,25OH2D3 on global gene expression in pancreatic islets.

Wolden-Kirk H, Overbergh L, Gysemans C, Brusgaard K, Naamane N, Van Lommel L, Schuit F, Eizirik DL, Christesen H, Mathieu C. Wolden-Kirk H, et al. Among authors: brusgaard k. J Steroid Biochem Mol Biol. 2013 Jul;136:68-79. doi: 10.1016/j.jsbmb.2012.10.017. Epub 2012 Nov 5. J Steroid Biochem Mol Biol. 2013. PMID: 23137852

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